Hangzhou Jimushi Meditech Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K222677 | Intermittent nelaton catheter for single use | April 5, 2023 |
| K200134 | Jimushi Sterile Urethral Catheter for single use | June 1, 2020 |